key: cord-0942019-y9tq7o0v authors: Liu, Qian; Dai, Yaping; Feng, Meimei; Wang, Xu; Liang, Wei; Yang, Fumeng title: Associations between serum amyloid A, interleukin‐6, and COVID‐19: A cross‐sectional study date: 2020-08-28 journal: J Clin Lab Anal DOI: 10.1002/jcla.23527 sha: 943e24c40b37400e2f608f3690187f6e83b0aeba doc_id: 942019 cord_uid: y9tq7o0v BACKGROUND: Serum amyloid A (SAA), interleukin‐6 (IL‐6) and neutrophil‐to‐lymphocyte ratio (NLR) play critical roles in inflammation and are used in clinical laboratories as indicators of inflammation‐related diseases. We aimed to provide potential laboratory basis for auxiliary distinguishing coronavirus disease (COVID‐19) by monitoring above indicators. METHODS: A total of 84 patients with confirmed COVID‐19 were enrolled in the study. Baseline characteristics and laboratory results were collected and analyzed. Receiver operating characteristic (ROC) curve analysis was used to combined detection of SAA and IL‐6 in patients with COVID‐19, and independent risk factors for severity of COVID‐19 were assessed by using binary logistic regression. RESULTS: The main clinical symptoms of patients with COVID‐19 were fever (98.8%), fatigue (61.9%), and dry cough (58.3%). SAA, IL‐6, and NLR were significantly higher in patients with COVID‐19 (all P < .001), and compared with nonsevere patients, three indicators of severe patients were significantly elevated. Besides, combined detection of SAA and IL‐6 better separates healthy people from patients with COVID‐19 than detection of SAA or IL‐6 alone. In addition, elevated SAA, IL‐6, and NLR can be used as independent variables for predicting the severity of patients with COVID‐19. CONCLUSION: Serum amyloid A and IL‐6 could be used as addition parameters to helping the distinguish of patients with COVID‐19 from healthy people, and can provide potential basis for separating patients with nonsevere and severe clinical signs. Coronaviruses mainly cause respiratory infections and some strains, such as severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), are associated with high infectivity and mortality, and thus are harmful to public health. 1, 2 In December 2019, pneumonia in people infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) appeared in Wuhan, Hubei Province. The infectious disease has since spread to other parts of the country and many overseas countries. [3] [4] [5] According to the official website of the Chinese Center for Disease continues to be reported. [6] [7] [8] [9] Existing reports show that approximately 84% of patients were categorized as nonsevere cases based on clinical symptoms, such as fever, cough, myalgia, or fatigue. [10] [11] [12] The rest of others were categorized as severe or critical cases which were mainly accompanied by acute respiratory distress syndrome (ARDS) or acute respiratory failure, and the median time from onset of symptoms to ARDS was about 9 days. [10] [11] [12] Besides, different types of patients often needed different plans of care, such as isolation for mild patients and intensive care units (ICU) for severe cases. Therefore, it is important to identify the risk factors of COVID-19 as early as possible so as to take appropriate interventions. Previous studies indicated that serum amyloid A (SAA) and interleukin-6 (IL-6) play important roles in viral diseases and were widely used in clinical laboratories as indicators of inflammation. [13] [14] [15] [16] [17] So far, the cytokine profile including IL-2, IL-6, IL-7, granulocyte colony-stimulating factor, interferon-γ, inducible protein 10, monocyte chemoattractant protein 1, macrophage inflammatory protein 1-α, and tumor necrosis factor-α has been considered to be associated with the severity of COVID-19. 18 In view of the above considerations, we aimed to provide potential laboratory basis for auxiliary distinguishing coronavirus disease (COVID-19) by detecting inflammation-related markers of SAA and IL-6. The white blood cell count, neutrophil count, lymphocyte count, red blood cell count, platelet count, and hemoglobin and C-reactive protein (CRP) levels were determined with a BC-5390 automatic hematology analyzer and associated reagents (Mindray Co., Ltd.). SAA was determined with commercially available assay kits (lot: 20190815, Zhuoyun Biotechnology Co., Ltd.) and an automatic biochemical analyzer (Beckman Co., Ltd.) by using the method of latex immunoturbidimetry. IL-6 was measured with a commercially available assay kit (lot: 921324, Beckman Co., Ltd.) and an Access 2 automatic immune analysis system (Beckman Co., Ltd.) by using the method of enzymelinked immunochemiluminescence. All equipment was maintained and calibrated according to the requirements. Internal quality control and external quality assessment were performed. From all subjects, 2 mL of EDTA K 2 anticoagulated venous blood was collected on admission for detection of the white blood cell count, neutrophil count, lymphocyte count, red blood cell count, platelet count, and hemoglobin and CRP levels. Meanwhile, 5 mL of venous blood (with a separation tube) was collected for the detection of SAA and IL-6. The latter specimens were centrifuged at 1200 × g for 10 minutes, and the detection of all analytes was completed within 4 hours. Data were analyzed in IBM SPSS Statistics 21.0, and data are expressed as median with interquartile range (IQR). The Mann-Whitney test was used to compare two independent groups. The Kruskal-Wallis test was used to compare multiple groups, and Dunnett's test was used for pairwise comparisons. Categorical variables were analyzed with chi-square test. The combined detection of laboratory indicators was analyzed with the receiver operating characteristic (ROC) curve, and risk factors were evaluated with binary logistic regression. A P value <.05 was considered statistically significant. The study included 84 hospitalized patients with COVID-19:59 were placed in the nonsevere group (mild and regular type), and 25 were placed in the severe group (severe and critical type) on admission. There was no statistical difference in the sex ratio, age, body mass index (BMI), and smoking status between the nonsevere group and severe group (P > .05). The median blood pressure (systolic pressure and diastolic pressure) in the two groups was significantly A significant difference was observed in lymphocyte count between patients with COVID-19 and healthy individuals. Lymphocyte count was significantly lower in patients with COVID-19, and it also showed a significant decrease in mild type patients (included in nonsevere group), but there was no statistical difference between the nonsevere group and the severe group. The levels of CRP were significantly higher in patients with severe disease than healthy controls and patients with nonsevere disease (P < .05). Moreover, the neutrophil-to-lymphocyte ratio (NLR), SAA, and IL-6 were significantly higher in patients with COVID-19 than in the healthy control group. In addition, the NLR, SAA, and IL-6 in patients were significantly higher in the severe group than in the nonsevere group (P < .05). Compared with healthy controls and nonsevere group, platelet-to lymphocyte-ratio (PLR) was significantly increased in severe group (P < .05). However, the white blood cell count, neutrophil count, red blood cell count, platelet count, and hemoglobin were not statistically different between healthy controls and patients with COVID-19 (Table 2, Figure 1 ). Based on the detection of nucleic acid as the gold standard for diagnosing COVID-19, and compared with SAA and IL-6, the ROC curve analysis showed that combined detection of SAA and IL-6 better separates healthy people from patients with COVID-19 than detection of SAA or IL-6 alone ( Figure 2 ). All patients with COVID-19 (nonsevere and severe group) were considered as dependent variables, and age, body mass index (BMI), (Table 3 ). Wuhan in December 2019 and was named by the WHO on January 12, 2020. It is the same genus as SARS-CoV and MERS-CoV, 21 and is extremely contagious, such that all people are susceptible. It is a cluster infectious disease and an outbreak occurred in the hospital. In severe cases, it can cause acute respiratory distress syndrome, multiple organ dysfunction, and even death. 22, 23 In this study, we ana- According to the novel coronavirus pneumonia diagnosis and treatment plan (trial version 7), 20 we divided 84 patients into a nonsevere group and a severe group. Retrospective analysis indicated that the blood pressure of patients with new severe disease was higher than that of patients with nonsevere disease, and there was a statistically significant difference between the two groups. The incidence of anorexia and dyspnea in patients with severe disease was significantly higher than that in those with nonsevere disease, and there was a statistically significant difference between the two groups. In addition, some patients still had some underlying diseases, such as diabetes, cardiovascular disease, cerebrovascular disease, chronic kidney disease, chronic obstructive pulmonary disease, or tumors, but there was no statistical difference in incidence between the two groups. A multicenter survey conducted by Guan et al 11 has shown that 23.7% of patients with COVID-19 have comorbidities, but the incidence of coexisting diseases was not statistically different between nonsevere and severe cases. Liu et al 26 have conducted a survey of 137 patients with COVID-19 and found that 19.7% of patients had coexisting diseases such as diabetes, cardiovascular disease, or hypertension, but the study did not compare the incidence of coexisting diseases between a nonsevere group and severe group. Although the above findings are consistent with those of this study, because the proportion of patients with COVID-19 with comorbidities is small, the current data cannot confirm whether there is a link between the severity of COVID-19 and comorbidities. We analyzed the results of laboratory indicators and found that the white blood cell count and neutrophil count of the patients with COVID-19 did not significantly differ, but the lymphocyte count was significantly lower than that in the healthy group. Moreover, the NLR of patients with COVID-19 was significantly higher than that of the healthy group, and it was higher in patients with severe disease. Meanwhile, our study also indicated that PLR was significantly higher in severe patients than that of healthy group and nonsevere patients. Similar to the above study, our research shows that IL-6 and inflammation indicators are significantly elevated in patients with COVID-19 and reflect the severity of the disease. Therefore, our study suggests that the expression levels of SAA and IL-6 in patients with COVID-19 should be detected as soon as possible, to provide an important laboratory basis for evaluating the severity of the disease. There are some limitations to this study. Firstly, because only 84 patients with COVID-19 were included, our conclusions must be further verified in more participants. Secondly, as patients come from different hospitals or regions, we have some difficulties in obtaining patient's data, which leads to incomplete acquire to some data, such as average time between infection and occurence of symptoms, the time from admission to the hospital and developing severe type, and part of laboratory indicators. Thirdly, this was a cross-sectional study, and we were unable to analyze the changes in laboratory indicators in patients in the treatment and prognosis stages; consequently, we lack corresponding information on the prognosis of the disease. Therefore, the changes in various indicators must be analyzed after treatment of patients to provide comprehensive reference values for disease prognosis. In conclusion, SAA and IL-6 could be used as addition parameters to helping the distinguish of patients with COVID-19 from healthy people, and can provide potential basis for separating patients with nonsevere and severe clinical signs. 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